115347-68-7 Usage
General Description
1H,1H,2H,2H-Heptafluoro-3,3-bis(trifluoromethyl)-1-iodohexane is a fluorinated compound with the chemical formula C7F14I. It is a liquid at room temperature and is commonly used as a solvent in chemical reactions and industrial processes. 1H,1H,2H,2H-HEPTAFLUORO-3,3-BIS(TRIFLUOROMETHYL)-1-IODOHEXANE is highly fluorinated, giving it strong chemical stability and resistance to heat and pressure. It also has a low dielectric constant, making it useful in electronic applications. However, it is important to handle this compound with care, as it is toxic and can be harmful if ingested or inhaled. Overall, 1H,1H,2H,2H-Heptafluoro-3,3-bis(trifluoromethyl)-1-iodohexane is a versatile chemical with a wide range of industrial and research applications.
Check Digit Verification of cas no
The CAS Registry Mumber 115347-68-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,3,4 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 115347-68:
(8*1)+(7*1)+(6*5)+(5*3)+(4*4)+(3*7)+(2*6)+(1*8)=117
117 % 10 = 7
So 115347-68-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H4F13I/c9-4(10,5(11,12)8(19,20)21)3(1-2-22,6(13,14)15)7(16,17)18/h1-2H2
115347-68-7Relevant articles and documents
NUCLEOPHILIC CATALYSIS OF THE ADDITION OF TERTIARY PERFLUOROALKYL BROMIDES TO ALKENES AND ALKYNES
Rozhkov, I. N.,Igumnov, S. M.,Pletnev, S. I.,Chaplina, I. V.
, p. 856 (2007/10/02)
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SYNTHESIS AND CHEMISTRY OF PERFLUORO-2-IODO-2-METHYL-ALKANES
Probst, A.,Raab, K.,Ulm, K.,Werner, K. von
, p. 223 - 246 (2007/10/02)
Two novel perfluoro-tert-alkyl iodides CF3(CF2)n+1C(CF3)2I have been obtained from F-alkenes CF3(CF2)n-CF=C(CF3)2 (n = 0 and 1) by formal additions of iodine fluoride; these required substantial alterations of known procedures.The F-tert-alkyl iodides are the most reactive alkyl halides known so far, and they are also very toxic.The following types of reactions have been studied: (a) Nucleophilic attack of anions at the iodine, leading to F-alkenes, (b) elimination of iodine fluoride, caused by metals or metal complexes, (c) pyrolysis, to give very selectively F-isobutene and n-perfluoroalkyl iodides, (d) photolysis, and (e) thermally induced insertions into the carbon-iodine bond.Screening results on the inhalation toxicity of the iodides and of some other fluoro-compounds are also reported.
